Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/20.500.12421/2050
Title: When serendipity knocks on the door: Synthesis and Physicochemical Characterization of 7-Chloro-2,3-dihydro-5H-thiazolo[3,2-a]pyrimidin-5-one
Authors: Carmona-Vargas, Christian C.
Ellena, Javier
D’Vries, Richard F.
Chaur, Manuel N.
Keywords: Chlorination
Serendipity
Thiazolopyrimidine
Thiobarbituric acid
Issue Date: 19-Mar-2019
Publisher: Sociedade Brasileira de Quimica
Abstract: Herein, we present the serendipitous obtaining of 7-chloro-2,3-dihydro-5H-thiazolo [3,2-a]pyrimidin-5-one in 40% yield by using POCl3 and a thiobarbituric acid derivative. The thiazolopyrimidine derivative was characterized by 1H nuclear magnetic resonance (NMR), UV-Vis, and Fourier transform infrared (FTIR) spectroscopy. Additionally, the structure was confirmed by single crystal X-ray diffraction, where it was found that the compound crystallizes in the P-1 triclinic space group with two conformeric molecules of 7-chloro-2,3-dihydro-5H-thiazolo [3,2-a]pyrimidin-5-one by asymmetric unit. Also, from the structural data was studied the supramolecular interactions using Hirshfeld surface analysis and 2D fingerprint plots. © 2019 Sociedade Brasileira de Química
URI: https://repository.usc.edu.co/handle/20.500.12421/2050
ISSN: 01035053
Appears in Collections:Artículos Científicos



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